29 results
·
29ms
·
Sources: EU EUDAMED, US FDA
SURGICAL INSTRUMENT GUIDE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VENTRALEX
FDA UDI
Davol Inc.·00801741031472·Ventralex ST Hernia Patch, 4.3 cm (1.7"), Circle
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169523869·MODULE 2950007 CANNULATED TAPS
Corin TriFit CF Hip Stem
FDA UDI
CORIN LTD·05056139231100·TriFit™ CF Rasp (Size 7)
Stealth Lingual
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746113819·COSMETIC BRACKET STEALTH LINGUAL MAND ANT/CSP 0...
ACOUSTIC OTOCOPE RECORDER
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Modified Bencox Hip System
FDA 510(k)
FDA Class 2
·Orthopedic
PROGRIP
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·October 28, 2019
PROGRIP
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·February 19, 2021
PROGRIP
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·June 18, 2021
PARIETEX
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·March 7, 2019
PROGRIP
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION SAS·Product code FTL·November 30, 2020
VENTRALEX ST
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·February 28, 2018
VENTRALEX ST
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·February 28, 2018
FRESENIUS 2008K
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 27, 2014
UNKNOWN ZIMMER IMPLANT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDI·February 6, 2013
CELL-DYN SAPPHIRE VENT HEAD ASSEMBLY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·January 6, 2011
VENTRALEX ST
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·December 7, 2018
BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024
MESH - SURGIPRO¿
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code FTL·August 6, 2018